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The Adipose Tissue Microenvironment Regulates Depot-Specific Adipogenesis in Obesity

机译:脂肪组织的微环境调节肥胖中特定于油库的脂肪形成。

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SUMMARY The sexually dimorphic distribution of adipose tissue influences the development of obesity-associated pathologies. The accumulation of visceral white adipose tissue (VWAT) that occurs in males is detrimental to metabolic health, while accumulation of subcutaneous adipose tissue (SWAT) seen in females may be protective. Here, we show that adipocyte hyperplasia contributes directly to the differential fat distribution between the sexes. In male mice, high-fat diet (HFD) induces adipogenesis specifically in VWAT, while in females HFD induces adipogenesis in both VWAT and SWAT in a sex hormone-dependent manner. We also show that the activation of adipocyte precursors (APs), which drives adipocyte hyperplasia in obesity, is regulated by the adipose depot microenvironment and not by cell-intrinsic mechanisms. These findings indicate that APs are plastic cells, which respond to both local and systemic signals that influence their differentiation potential independent of depot origin. Therefore, depot-specific AP niches coordinate adipose tissue growth and distribution.
机译:发明内容脂肪组织的有性二态分布影响肥胖相关病理的发展。男性内脏白色脂肪组织(VWAT)的积累对代谢健康有害,而女性中皮下脂肪组织(SWAT)的积累可能具有保护作用。在这里,我们显示脂肪细胞增生直接促进了两性之间的脂肪分布差异。在雄性小鼠中,高脂饮食(HFD)在VWAT中特异性诱导脂肪形成,而在雌性动物中,HFD以性激素依赖性方式在VWAT和SWAT中诱导脂肪形成。我们还显示,在肥胖症中驱动脂肪细胞增生的脂肪细胞前体(APs)的激活受脂肪库微环境的调节,而不是受细胞内在机制的调节。这些发现表明,AP是可塑性细胞,对局部信号和系统信号均具有响应,这些信号会影响其分化潜能,而与储库来源无关。因此,特定于仓库的AP小生境协调脂肪组织的生长和分布。

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